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Fig 1.

(A) SEM Microscopy SEM 10000x 15 kV FTO-GLAS Clean, FTO-GLASS EDX Analysis (B) Microscopy SEM 10000x 15 kV FTO-GLAS-APTES with their respective diffraction in FTO- GLAS-APTES; (C). Microscopy SEM 10000x 15 kV FTO-GLASS-APTES-PDITC and Diffraction; (D). Microscopy SEM 10000x 15 kV FTO-GLAS-APTES-PDITC-DNA and diffraction.

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Fig 1 Expand

Fig 2.

Raman shift of interaction with each monolayer; FTO-nude, this the first step for modification of the sensor, followed by monolayers of APTES, PDITC and DNA, showing an interaction between them demonstrating adequate coupling.

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Fig 2 Expand

Fig 3.

(A) Voltagrams of each stage of immobilization in an electrochemical cell with a three-electrode configuration; Reference electrode (Ag / AgCl 1.0 M), Counter-electrode (Platinum), Working electrode (FTO-MODIFIED) Ferri / Ferro 0.1 M in Buffer PBS 0.1 M, in a potential window -0.400 to 1.100 V, at a rate of 100 mV/s. (B) Voltagrams of the different scanning rates using the FTO-DNA capture electrode, ranging from 10 mV/s to 250 mV/s.

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Fig 3 Expand

Fig 4.

Sensor response represented by the behavior of the absolute value of the cathodic peaks towards samples without synthetic DNA (BLANK), samples with 50nM of non-complementary synthetic DNA sequence and samples with 50nM of complementary synthetic DNA sequence.

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Fig 4 Expand

Fig 5.

Sensor calibration curve using the absolute value of cathodic current peak versus target DNA concentration in a range 1 nM to 500 nM, showing a logarithmic trend.

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Fig 5 Expand

Fig 6.

Sensor calibration curve using the absolute value of cathodic current peak versus target DNA concentration in range 1nM to 100nM, showing a lineal trend.

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Fig 6 Expand

Fig 7.

(A) Ratio of the sample signal (DNA) divided by the baseline signal (EA) of the concentrations, 160 ng/mL (2.00x10-2), 0.016 ng/mL (2.00x10-6), 0.00016 ng/mL (2.00x10-8) and 0. 0.000016 ng/mL (2.00x10-9). (B) 12% acrylamide gel of the PCR amplicons at dilutions 1 (2.00x10-2), 2 (2.00x10-6), 3 (2.00x10-8) and 4 (2.00x10-9).

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Fig 7 Expand

Fig 8.

(A) Three "Spikes" urines were evaluated containing 100 ng, 1 ng, 10 pg, 100 fg and 1 fg of MTB DNA. It was compared with real time PCR.

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Fig 8 Expand

Fig 9.

The response ratio of the sputum samples according to the bacillary load presented in the sputum smear (BK).

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Fig 9 Expand